Lactulose Solution
Product Images NDC 83745-249

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Lactulose (NDC 83745-249). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apozeal Pharmaceuticals Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Containerlabel16oz (Containerlabel16oz)

Lactulose Solution, USP 10 g/15 mL oral and rectal solution label by Apozeal Pharmaceuticals Inc. The 16 fl oz (473 mL) bottle label shows dosage form and strength, usage indication for portal-systemic encephalopathy, handling instructions, and a barcode. The label includes the manufacturer info and is marked Rx only.*

FDA Label Image

Containerlabel32oz (Containerlabel32oz)

Label for Lactulose Solution, USP oral and rectal solution, 10 g per 15 mL, manufactured by Apozeal Pharmaceuticals Inc. The label includes dosage form, strength, route, volume of 32 fl oz (946 mL), and storage instructions. It also states the solution is for prescription use and provides the NDC 83745-249-32.*

FDA Label Image

Containerlabel8oz (Containerlabel8oz)

Lactulose Solution, USP oral and rectal administration, 10 g/15 mL, in an 8 fl. oz (237 mL) container. The label states it is prescription only and manufactured by Apozeal Pharmaceuticals Inc. The label includes storage instructions, dosage information, and a barcode on the side.*

FDA Label Image

Logo (Logo)

FDA Label Image

Structure (Structure)

Chemical structure of lactulose, showing the molecular arrangement of its sugar components with hydroxyl groups and oxygen atoms forming ring structures.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.